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Equipment Validation Engineer

Job in Round Lake, Lake County, Illinois, 60073, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Biomedical Engineer, Validation Engineer, Quality Engineering, Systems Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Job Summary

Lab Equipment Validation Engineer responsible for leading validation activities for laboratory equipment supporting infusion system testing in a regulated medical device environment, ensuring compliance with FDA regulations, ISO standards, and quality system requirements.

Roles & Responsibilities
  • Lead validation efforts for laboratory equipment supporting infusion system testing (e.g., Infuscale, altitude chambers, environmental chambers, flow measurement instruments, and related test systems).
  • Develop and execute validation protocols, test plans, and reports in alignment with FDA 21 CFR Part 820, Part 11, ISO 13485, and equipment validation best practices.
  • Partner with R&D, Quality, and Systems Engineering teams to define equipment validation requirements and risk based strategies.
  • Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution.
  • Ensure validated equipment supports all infusion system verification needs including flow accuracy, environmental stress testing, and performance simulation.
  • Collaborate with hardware, firmware, and systems engineering teams to ensure equipment suitability and proper test coverage.
  • Investigate and resolve equipment issues discovered during validation or testing activities.
  • Support calibration, maintenance, and lifecycle management of lab equipment used for infusion system tests.
  • Drive continuous improvement of validation processes, documentation quality, and lab test methodologies.
  • Maintain accurate and compliant documentation per Baxter quality systems, design control, and equipment lifecycle standards.
Education & Experience
  • Bachelor's or Master's degree in Electrical Engineering, Biomedical Engineering, Mechanical Engineering, Computer Engineering, or related technical field.
  • Minimum 5+ years of experience in equipment validation or software validation within a medical device or FDA regulated environment.
  • Strong understanding of FDA regulations, ISO 13485, equipment validation, and regulated testing processes. Hands on experience with lab equipment used in infusion system testing:
    Infuscale, altitude chambers, environmental chambers, flow measurement instruments, and similar test systems.
  • Experience with tools such as LabVIEW or Python for automating test data acquisition (as applicable).
  • Hands on experience with test measurement instruments such as temperature chambers, flow analyzers, pressure sensors, oscilloscopes, and calibration tools.
  • Understanding of risk management frameworks (ISO 14971).
  • Experience working within formal document control, change management, and validation documentation systems.
  • Prior experience validating lab equipment specifically for infusion systems or drug delivery devices.
  • Knowledge of environmental and stress testing methodologies for medical device performance verification.
  • Familiarity with data integrity and cybersecurity considerations in lab test environments.
  • Certifications such as CSQE, CMII, or Lean Six Sigma are a plus.
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